Hyperbilirubinemia

S
Shini CherianRegistered nurse um MOI
HYPERBILIRUBINEMIA
Shini Cherian ,
NESD,
SFHD.
OBJECTIVES
Define Hyperbilirubinemia
State causes of hyperbilirubinemia.
 Discuss the pathophysiology of
hyperbilirubinemia.
Describe the most dangerous complication
of hyperbilirubinemia.
List the three elements of therapeutic
management.
Design plan of care for baby has
hyperbilirubinemia.
DEFINITION
Hyperbilirubinemia refers to an
excessive level of accumulated bilirubin
in the blood and is characterized by
jaundice, a yellowish discoloration of the
skin, sclera, mucous membranes and
nails.
Unconjugated bilirubin = Indirect bilirubin.
Conjugated bilirubin = Direct bilirubin.
INCIDENCE
Term : 60% of term neonates
Preterm : 80% of preterm neonates
Risk factors for jaundice
JAUNDICE
• J - jaundice within first 24 hrs. of life
• A - a sibling who was jaundiced as neonate
• U - unrecognized hemolysis
• N – non-optimal sucking/nursing
• D - deficiency of G6PD
• I - infection
• C – Cephalhematoma /bruising
• E - East Asian/North Indian
PATHOPHYSIOLOGY
Hyperbilirubinemia
Hyperbilirubinemia
Hyperbilirubinemia
MECHANISMS OF NEONATAL
JAUNDICE
1.Increased Bilirubin Load due to a high
hemoglobin concentration.
• The normal newborn infant
• Hemolysis
• Cephalhematoma or bruising , Polycythemia
2. Decreased Bilirubin Conjugation in the liver
• Decreased uridine glucuronyl transferase Activity
• Glucuronyl Transferase Deficiency Type 1 (Crigler
Najar Syndrome)
3. Defective Bilirubin Excretion
TYPES OF BILIRUBIN
Physiological jaundice
Characteristics
• Appears after 24 hours
• Maximum intensity by 4th-5th day in term
& 7th day in preterm
• Serum level less than 15 mg / dl
• Clinically not detectable after 14 days
• Disappears without any treatment
Pathological jaundice
Appears within 24 hours of age
• Increase of bilirubin > 5 mg / dl / day
• Serum bilirubin > 15 mg / dl
• Jaundice persisting after 14 days
• Stool clay / white colored and urine staining
clothes yellow
• Direct bilirubin> 2 mg / dl
Hyperbilirubinemia
Hyperbilirubinemia
Clinical assessment of
Jaundice
Hyperbilirubinemia
MANAGEMENT
Hyperbilirubinemia
Hyperbilirubinemia
Hyperbilirubinemia
Hyperbilirubinemia
Hyperbilirubinemia
Hyperbilirubinemia
Hyperbilirubinemia
Intensive Phototherapy
Hyperbilirubinemia
Hyperbilirubinemia
Hyperbilirubinemia
EXCHANGE BLOODEXCHANGE BLOOD
TRANSFUSIONTRANSFUSION
Hyperbilirubinemia
In single volume exchange (in severe
neonatal anemia): A suggested rateis15 aliquotsover 1
hour that is, 4 minuteseach cycle.
Aliqoutvolume(ml)= estimatedbloodvolumexinfantweight(kg)/
numberof aliquots in1hour= 85mlxweight(kg)Itis usually
5ml/kg
In double volume exchange: A suggested rate
is 30 aliquots over2 hours that is, 4 minutes each cycle. This
is irrespective of whetherthe isovolumetric orpush-pull
method is used.
Aliqoutvolume(ml)= estimatedbloodvolumex2xinfantweight
(kg)/numberof aliquots in2hours = 85mlx2xweight(kg)itis
usually5ml/kg.
Rate of transfusion
Hyperbilirubinemia
Isovolumetric exchange- access is via
an umbilical venous catheter(blood in)
and an umbilical arterial catheter(blood
out).
Push pull method- using same catheter
that is the blood are pushed in pulled out
through the same umbilical venous
catheter.
ISOVOLUMETRIC METHODISOVOLUMETRIC METHOD
Hyperbilirubinemia
PUSH-PULL METHODPUSH-PULL METHOD
Hyperbilirubinemia
Hyperbilirubinemia
Hyperbilirubinemia
Hyperbilirubinemia
 Check the patients chart forsigned exchanged transfusion order
 Check consent form signed by parents
 Ensure exchange blood unit is available in the blood bank and have it brought to area just prior
to procedure.
 Obtain received amount of blood from blood bank. Double check the blood pack with another
nurse to ensure correct identification.
 Equipment forumbilical catheterization must be available including:
 Clean equipment sterile equipment
 Clean dressing trolley, blue sterile plastic sheet to place understerile drape
 IV infusion pump
 Blood warmer
 3.0 silk suture, sterile linen, cord tie, scalpel blade, tape measure
 PPElike: masks protective goggles, sterile gown, two sets of sterile gloves, sterile green
drapes, sterile dressing, additional gauze swabs, assorted needles/5 ml syringes
 heparinized saline
 Unopened solutions forskin preparation(aqueous chlorhexidine)
 UVC 5 Finfants 1000g and <28 weeks and 3.5 Finfants <1000g or>28weeks
 Prepare the infant fortransfusion, afterchecking the identification band, keep NPO, Evacuate
gastric contents through a 8G=FG feeding tube and leave on free drainage; obtain baseline vital
signs and blood pressure.
 Infants > 34weeks gestation are placed on servo mode but < 34weeks are managed in isollete.
 Access forprocedure: insertion of 5 FG umbilical catheterby physician to a level that allows free
flowing withdrawal of blood
 Patient should be on continuous cardiac monitoring
 Secure the infant’s upperand lowerextremities as perrestraint policy
 Maintain the infant’s temperature with radiant warmeron servo control, take the infant’s
temperature at least hourly oras ordered
Standard precautions and aseptic technique should be
taken
The physician will connect the umbilical catheterto the
first adaptoron the 4-ways stopcock
 Take a 20cc syringe from the tray, and attach to the
second adaptoron the way stopcock
Attach the blood administration set with extension tubing
to the third adaptoron the 4-way stopcock
 Connect the remaining adaptorof the 4-way stopcock to
the waste blood containerand secure properly below the
table level
Draw pre-exchange laboratory work including dextrose
stick
 The nurse must observe the infant and record the amount
of blood out and amount of the blood in and time
 Document heart rate, respiratory and blood pressure
every 5 minutes and inform physician of any changes in
the vital signs
Blood Specimens
Initial or “First Out”.
 FBC & film.
 Blood Group, Direct Coomb's test.
 Urea and electrolytes, calcium, SBR, total and conjugated.
 Blood gas with PGL.
 Coagulations profile.
 Newborn screening test.
 Hold samples for other tests as indicated, e.g. G6PD deficiency, viral infection,
hereditary spherocytosis, metabolic studies.
Halfway Specimens
 SBR
 Blood gas with PGL
 FBC/Coagulation screen if warranted
End or “Last Out” specimens
 SBR, Urea & Electrolytes, calcium, magnesium, phosphate.
 FBC and Cross match for possible subsequent exchange.
 Coagulation studies.
 Blood gas with PGL
Post Exchange
Measure serum bilirubin within 2 hours
NICU Exchange Transfusion Chart
Date : Aliquots (circle one):
5 ml 10 ml 20 ml
Total
volume
to be
infused:
Vital signs
Cycle Time Volume out Total
out
Volume in Total in HR RE BP T SPO2 BSL
Sample
for lab.
Medications
1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
11.
12.
13.
14.
15.
Total
 Infection
 Vascularcomplication
 Coagulopathies
 Electrolytes abnormalities
 Metabolic alkalosis
 Necrotizing Enterocolitis
QUESTIONSQUESTIONS
ANSWERSANSWERS
ANSWERSANSWERS
QUESTIONSQUESTIONS
Hyperbilirubinemia
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Hyperbilirubinemia

  • 2. OBJECTIVES Define Hyperbilirubinemia State causes of hyperbilirubinemia.  Discuss the pathophysiology of hyperbilirubinemia. Describe the most dangerous complication of hyperbilirubinemia. List the three elements of therapeutic management. Design plan of care for baby has hyperbilirubinemia.
  • 3. DEFINITION Hyperbilirubinemia refers to an excessive level of accumulated bilirubin in the blood and is characterized by jaundice, a yellowish discoloration of the skin, sclera, mucous membranes and nails. Unconjugated bilirubin = Indirect bilirubin. Conjugated bilirubin = Direct bilirubin.
  • 4. INCIDENCE Term : 60% of term neonates Preterm : 80% of preterm neonates
  • 5. Risk factors for jaundice JAUNDICE • J - jaundice within first 24 hrs. of life • A - a sibling who was jaundiced as neonate • U - unrecognized hemolysis • N – non-optimal sucking/nursing • D - deficiency of G6PD • I - infection • C – Cephalhematoma /bruising • E - East Asian/North Indian
  • 10. MECHANISMS OF NEONATAL JAUNDICE 1.Increased Bilirubin Load due to a high hemoglobin concentration. • The normal newborn infant • Hemolysis • Cephalhematoma or bruising , Polycythemia 2. Decreased Bilirubin Conjugation in the liver • Decreased uridine glucuronyl transferase Activity • Glucuronyl Transferase Deficiency Type 1 (Crigler Najar Syndrome) 3. Defective Bilirubin Excretion
  • 12. Physiological jaundice Characteristics • Appears after 24 hours • Maximum intensity by 4th-5th day in term & 7th day in preterm • Serum level less than 15 mg / dl • Clinically not detectable after 14 days • Disappears without any treatment
  • 13. Pathological jaundice Appears within 24 hours of age • Increase of bilirubin > 5 mg / dl / day • Serum bilirubin > 15 mg / dl • Jaundice persisting after 14 days • Stool clay / white colored and urine staining clothes yellow • Direct bilirubin> 2 mg / dl
  • 32. In single volume exchange (in severe neonatal anemia): A suggested rateis15 aliquotsover 1 hour that is, 4 minuteseach cycle. Aliqoutvolume(ml)= estimatedbloodvolumexinfantweight(kg)/ numberof aliquots in1hour= 85mlxweight(kg)Itis usually 5ml/kg In double volume exchange: A suggested rate is 30 aliquots over2 hours that is, 4 minutes each cycle. This is irrespective of whetherthe isovolumetric orpush-pull method is used. Aliqoutvolume(ml)= estimatedbloodvolumex2xinfantweight (kg)/numberof aliquots in2hours = 85mlx2xweight(kg)itis usually5ml/kg.
  • 35. Isovolumetric exchange- access is via an umbilical venous catheter(blood in) and an umbilical arterial catheter(blood out). Push pull method- using same catheter that is the blood are pushed in pulled out through the same umbilical venous catheter.
  • 43.  Check the patients chart forsigned exchanged transfusion order  Check consent form signed by parents  Ensure exchange blood unit is available in the blood bank and have it brought to area just prior to procedure.  Obtain received amount of blood from blood bank. Double check the blood pack with another nurse to ensure correct identification.  Equipment forumbilical catheterization must be available including:  Clean equipment sterile equipment  Clean dressing trolley, blue sterile plastic sheet to place understerile drape  IV infusion pump  Blood warmer  3.0 silk suture, sterile linen, cord tie, scalpel blade, tape measure  PPElike: masks protective goggles, sterile gown, two sets of sterile gloves, sterile green drapes, sterile dressing, additional gauze swabs, assorted needles/5 ml syringes  heparinized saline  Unopened solutions forskin preparation(aqueous chlorhexidine)  UVC 5 Finfants 1000g and <28 weeks and 3.5 Finfants <1000g or>28weeks  Prepare the infant fortransfusion, afterchecking the identification band, keep NPO, Evacuate gastric contents through a 8G=FG feeding tube and leave on free drainage; obtain baseline vital signs and blood pressure.  Infants > 34weeks gestation are placed on servo mode but < 34weeks are managed in isollete.  Access forprocedure: insertion of 5 FG umbilical catheterby physician to a level that allows free flowing withdrawal of blood  Patient should be on continuous cardiac monitoring  Secure the infant’s upperand lowerextremities as perrestraint policy  Maintain the infant’s temperature with radiant warmeron servo control, take the infant’s temperature at least hourly oras ordered
  • 44. Standard precautions and aseptic technique should be taken The physician will connect the umbilical catheterto the first adaptoron the 4-ways stopcock  Take a 20cc syringe from the tray, and attach to the second adaptoron the way stopcock Attach the blood administration set with extension tubing to the third adaptoron the 4-way stopcock  Connect the remaining adaptorof the 4-way stopcock to the waste blood containerand secure properly below the table level Draw pre-exchange laboratory work including dextrose stick  The nurse must observe the infant and record the amount of blood out and amount of the blood in and time  Document heart rate, respiratory and blood pressure every 5 minutes and inform physician of any changes in the vital signs
  • 45. Blood Specimens Initial or “First Out”.  FBC & film.  Blood Group, Direct Coomb's test.  Urea and electrolytes, calcium, SBR, total and conjugated.  Blood gas with PGL.  Coagulations profile.  Newborn screening test.  Hold samples for other tests as indicated, e.g. G6PD deficiency, viral infection, hereditary spherocytosis, metabolic studies. Halfway Specimens  SBR  Blood gas with PGL  FBC/Coagulation screen if warranted End or “Last Out” specimens  SBR, Urea & Electrolytes, calcium, magnesium, phosphate.  FBC and Cross match for possible subsequent exchange.  Coagulation studies.  Blood gas with PGL Post Exchange Measure serum bilirubin within 2 hours
  • 46. NICU Exchange Transfusion Chart Date : Aliquots (circle one): 5 ml 10 ml 20 ml Total volume to be infused: Vital signs Cycle Time Volume out Total out Volume in Total in HR RE BP T SPO2 BSL Sample for lab. Medications 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13. 14. 15. Total
  • 47.  Infection  Vascularcomplication  Coagulopathies  Electrolytes abnormalities  Metabolic alkalosis  Necrotizing Enterocolitis